ClearanceBrief
510(k) K091257 ยท FCG Biopsy Needle

MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM

ApplicantMedi-Globe Corporation, Tempe AZ, US
DecisionSubstantially Equivalent, May 8, 2009
ReceivedApr 29, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091257

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.